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1440522-03-1

C40H67FN10O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1440522-03-1 Structure

  • Basic information

    1. Product Name: C40H67FN10O8
    2. Synonyms:
    3. CAS NO:1440522-03-1
    4. Molecular Formula:
    5. Molecular Weight: 835.033
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1440522-03-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C40H67FN10O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C40H67FN10O8(1440522-03-1)
    11. EPA Substance Registry System: C40H67FN10O8(1440522-03-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1440522-03-1(Hazardous Substances Data)

1440522-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440522-03-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,5,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1440522-03:
(9*1)+(8*4)+(7*4)+(6*0)+(5*5)+(4*2)+(3*2)+(2*0)+(1*3)=111
111 % 10 = 1
So 1440522-03-1 is a valid CAS Registry Number.

1440522-03-1Downstream Products

1440522-03-1Relevant articles and documents

Impact of the Proline Residue on Ligand Binding of Neurotensin Receptor2 (NTS2)-Selective Peptide-Peptoid Hybrids

Held, Cornelia,Huebner, Harald,Kling, Ralf,Nagel, Yvonne A.,Wennemers, Helma,Gmeiner, Peter

supporting information, p. 772 - 778 (2013/08/25)

To investigate the binding mode and structure-activity relationships (SARs) of selective neurotensin receptor2 (NTS2) ligands, novel peptide-peptoid hybrids that simulate the function of the endogenous ligand were developed. Starting from our recently described NTS2 ligands of type 1, structural variants of type 2 and the metabolically stable analogues 3a,b were developed. Replacement of the proline unit by a collection of structural surrogates and evaluation of the respective molecular probes for NTS2 affinity and selectivity indicated similar SARs as described for NT(8-13) derivatives bound to the subtype NTS1. Peptide-peptoid hybrids 2d, 3a,b showed substantial NTS2 binding affinity (Ki=8.1-16nM) and 2400-8600-fold selectivity over NTS1. The thiazolidine derivative 3b showed metabolic stability over 32h in a serum degradation assay. In an inositol phosphate accumulation assay, the neurotensin mimetics 3a and 3b displayed an inhibition of constitutive activity exceeding 1.7-2.0times the activity of NT(8-13). The fluorinated derivative 3a could afford attractive opportunities to detect NTS2 by 19F magnetic resonance imaging.

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